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(PaAP)的分泌性氨肽酶。

The Secreted Aminopeptidase of (PaAP).

机构信息

Maurice and Gabriela Goldschleger Eye Research Institute, Faculty of Medicine and Health Sciences, Sheba Medical Center, Tel Aviv University, Ramat-Gan 5262000, Israel.

出版信息

Int J Mol Sci. 2024 Aug 2;25(15):8444. doi: 10.3390/ijms25158444.

DOI:10.3390/ijms25158444
PMID:39126017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11313473/
Abstract

is an opportunistic pathogen that causes severe infections in compromised hosts. infections are difficult to treat because of the inherent ability of the bacteria to develop antibiotic resistance, secrete a variety of virulence factors, and form biofilms. The secreted aminopeptidase (PaAP) is an emerging virulence factor, key in providing essential low molecular weight nutrients and a cardinal modulator of biofilm development. PaAP is therefore a new potential target for therapy of infections. The present review summarizes the current knowledge of PaAP, with special emphasis on its biochemical and enzymatic properties, activation mechanism, biological roles, regulation, and structure. Recently developed specific inhibitors and their potential as adjuncts in the treatment of infections are also described.

摘要

是一种机会性病原体,可导致机体免疫功能低下者发生严重感染。由于细菌固有产生抗生素耐药性、分泌多种毒力因子并形成生物膜的能力, 感染的治疗较为困难。分泌的氨肽酶(PaAP)是一种新兴的毒力因子,为提供必需的低分子量营养物质和生物膜形成的主要调节剂。因此,PaAP 是 感染治疗的新潜在靶点。本文综述了 PaAP 的最新研究进展,特别强调了其生化和酶学特性、激活机制、生物学作用、调控和结构。还描述了最近开发的特异性抑制剂及其作为 感染辅助治疗的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/11313473/fecae2e0cddf/ijms-25-08444-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/11313473/0f8a7fad3c4c/ijms-25-08444-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/11313473/305a2895b20d/ijms-25-08444-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/11313473/fecae2e0cddf/ijms-25-08444-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/11313473/0f8a7fad3c4c/ijms-25-08444-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/11313473/305a2895b20d/ijms-25-08444-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69bf/11313473/fecae2e0cddf/ijms-25-08444-g003.jpg

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Dipeptidic Phosphonates: Potent Inhibitors of Pseudomonas aeruginosa Elastase B Showing Efficacy in a Murine Keratitis Model.二肽基膦酸盐:铜绿假单胞菌弹性蛋白酶B的强效抑制剂,在小鼠角膜炎模型中显示出疗效。
Adv Sci (Weinh). 2025 Apr;12(14):e2411807. doi: 10.1002/advs.202411807. Epub 2025 Feb 19.
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